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Journal of Neurology, Neurosurgery, and Psychiatry
|
September 1, 1988
Carnitine palmitoyltransferase deficiency
L A Bindoff, H S Sherratt, R Singh, et al.
Acta Neurologica Scandinavica. Supplementum
|
April 11, 2007
Clinical evolution of Kearns-Sayre syndrome with polyendocrinopathy and respiratory failure
P S Sanaker, E S Husebye, O Fondenes, et al.
Acta Neurologica Scandinavica. Supplementum
|
July 2, 2009
Mitochondrial DNA depletion in progressive external ophthalmoplegia caused by POLG1 mutations
C Tzoulis, M Papingji, T Fiskestrand, et al.
Journal of the Royal Society of Medicine
|
April 1, 1995
The investigation of mitochondrial respiratory chain disease
A A Morris, M J Jackson, L A Bindoff, et al.
Biochemical and Biophysical Research Communications
|
October 15, 1993
An antisense oligodeoxynucleotide approach to investigate the function of the nuclear-encoded subunits of human cytochrome c oxidase
Z M Chrzanowska-Lightowlers, D M Turnbull, L A Bindoff, et al.
Neurology
|
November 14, 2008
A novel Refsum-like disorder that maps to chromosome 20
T Fiskerstrand, P Knappskog, J Majewski, et al.
Cerebellum (London, England)
|
May 12, 2016
PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
C Tzoulis, Paweł Sztromwasser, Stefan Johansson, et al.
Annals of Neurology
|
November 1, 1990
Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiency
L Farnsworth, I M Shepherd, M A Johnson, et al.
Gene
|
April 27, 1999
Conversion of a reporter gene for mitochondrial gene expression using iterative mega-prime PCR
Z M Chrzanowska-Lightowlers, R J Temperley, A McGregor, et al.
Neurology
|
December 28, 2006
Unusual features in a boy with the rapsyn N88K mutation
G O Skeie, H Aurlien, J S Müller, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 58) with videos related to
Sort By:
Page
of 6
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 1, 1988
Carnitine palmitoyltransferase deficiency
L A Bindoff, H S Sherratt, R Singh, et al.
Acta Neurologica Scandinavica. Supplementum
|
April 11, 2007
Clinical evolution of Kearns-Sayre syndrome with polyendocrinopathy and respiratory failure
P S Sanaker, E S Husebye, O Fondenes, et al.
Acta Neurologica Scandinavica. Supplementum
|
July 2, 2009
Mitochondrial DNA depletion in progressive external ophthalmoplegia caused by POLG1 mutations
C Tzoulis, M Papingji, T Fiskestrand, et al.
Journal of the Royal Society of Medicine
|
April 1, 1995
The investigation of mitochondrial respiratory chain disease
A A Morris, M J Jackson, L A Bindoff, et al.
Biochemical and Biophysical Research Communications
|
October 15, 1993
An antisense oligodeoxynucleotide approach to investigate the function of the nuclear-encoded subunits of human cytochrome c oxidase
Z M Chrzanowska-Lightowlers, D M Turnbull, L A Bindoff, et al.
Neurology
|
November 14, 2008
A novel Refsum-like disorder that maps to chromosome 20
T Fiskerstrand, P Knappskog, J Majewski, et al.
Cerebellum (London, England)
|
May 12, 2016
PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
C Tzoulis, Paweł Sztromwasser, Stefan Johansson, et al.
Annals of Neurology
|
November 1, 1990
Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiency
L Farnsworth, I M Shepherd, M A Johnson, et al.
Gene
|
April 27, 1999
Conversion of a reporter gene for mitochondrial gene expression using iterative mega-prime PCR
Z M Chrzanowska-Lightowlers, R J Temperley, A McGregor, et al.
Neurology
|
December 28, 2006
Unusual features in a boy with the rapsyn N88K mutation
G O Skeie, H Aurlien, J S Müller, et al.
Page
of 6